Morton D J, Whitby P W, Jin H, Ren Z, Stull T L
Departments of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.
Infect Immun. 1999 Jun;67(6):2729-39. doi: 10.1128/IAI.67.6.2729-2739.1999.
Haemophilus influenzae requires heme for growth and can utilize hemoglobin and hemoglobin-haptoglobin as heme sources. We previously identified two hemoglobin- and hemoglobin-haptoglobin-binding proteins, HgpA and HgpB, in H. influenzae HI689. Insertional mutation of hgpA and hgpB, either singly or together, did not abrogate the ability to utilize or bind either hemoglobin or the hemoglobin-haptoglobin complex. A hemoglobin affinity purification method was used to isolate a protein of approximately 120 kDa from the hgpA hgpB double mutant. We have cloned and sequenced the gene encoding this third hemoglobin/hemoglobin-haptoglobin binding protein and designate it hgpC. Insertional mutation of hgpC did not affect the ability of the strain to utilize either hemoglobin or hemoglobin-haptoglobin. An hgpA hgpB hgpC triple mutant constructed by insertional mutagenesis showed a reduced ability to use the hemoglobin-haptoglobin complex but was unaltered in the ability to use hemoglobin. A second class of mutants was constructed in which the entire structural gene of each of the three proteins was deleted. The hgpA hgpB hgpC complete-deletion triple mutant was unable to utilize the hemoglobin-haptoglobin complex and showed a reduced ability to use hemoglobin. We have identified three hemoglobin/hemoglobin-haptoglobin-binding proteins in Haemophilus influenzae. Any one of the three proteins is sufficient to support growth with hemoglobin-haptoglobin as the heme source, and expression of at least one of the three is essential for hemoglobin-haptoglobin utilization. Although the three proteins play a role in hemoglobin utilization, an additional hemoglobin acquisition mechanism(s) exists.
流感嗜血杆菌生长需要血红素,并且能够利用血红蛋白和血红蛋白-触珠蛋白复合物作为血红素来源。我们之前在流感嗜血杆菌HI689中鉴定出两种血红蛋白和血红蛋白-触珠蛋白结合蛋白,即HgpA和HgpB。单独或共同对hgpA和hgpB进行插入突变,并未消除利用或结合血红蛋白或血红蛋白-触珠蛋白复合物的能力。采用血红蛋白亲和纯化方法从hgpA hgpB双突变体中分离出一种约120 kDa的蛋白质。我们已经克隆并测序了编码这种第三种血红蛋白/血红蛋白-触珠蛋白结合蛋白的基因,并将其命名为hgpC。hgpC的插入突变并不影响该菌株利用血红蛋白或血红蛋白-触珠蛋白的能力。通过插入诱变构建的hgpA hgpB hgpC三突变体利用血红蛋白-触珠蛋白复合物的能力降低,但利用血红蛋白的能力未改变。构建了第二类突变体,其中三种蛋白质的每个结构基因都被删除。hgpA hgpB hgpC完全缺失三突变体无法利用血红蛋白-触珠蛋白复合物,利用血红蛋白的能力也降低。我们在流感嗜血杆菌中鉴定出三种血红蛋白/血红蛋白-触珠蛋白结合蛋白。这三种蛋白质中的任何一种都足以支持以血红蛋白-触珠蛋白作为血红素来源的生长,并且三种蛋白中至少有一种的表达对于利用血红蛋白-触珠蛋白至关重要。尽管这三种蛋白质在利用血红蛋白方面发挥作用,但还存在另外一种血红蛋白获取机制。